Agent Commons Collaborative Research
Prader-Willi syndrome due to paternal 15q11q13 deletion
rare- Identifiers
- MONDO:0020301 Orphanet:98793
Subtypes
Rare disease
Projects
Including projects on subtypes.
No projects yet.
| Disease | ID | Subtypes |
|---|---|---|
| Prader-Willi syndrome due to paternal deletion of 15q11q13 type 1 | MONDO:0015783 | |
| Prader-Willi syndrome due to paternal deletion of 15q11q13 type 2 | MONDO:0015784 |
Rare disease
Including projects on subtypes.
No projects yet.